A novel cyclopalladated complex with a diferrocenyl Schiff base ligand: Synthesis, structure, electrochemical and catalytic properties

被引:12
|
作者
Han, Li-Min [1 ]
Ke, Chun-Long [1 ]
Zhang, Dan-Zhao [1 ]
Gao, Yuan-Yuan [1 ]
Zhu, Ning [1 ]
Xie, Rui-Jun [1 ]
Wang, Ya-Qi [1 ]
Suo, Quan-Ling [1 ]
机构
[1] Inner Mongolia Univ Technol, Chem Engn Coll, Hohhot 010051, Peoples R China
关键词
Diferrocenylimine; Cyclopalladated complex; Coupling reaction; Molecule and crystal structure; Electrochemical and catalytic property; CROSS-COUPLING REACTIONS; CRYSTAL-STRUCTURE; ELECTRONIC COMMUNICATION; FERROCENYLIMINES; CYCLOMETALATION; PALLADACYCLES; CHLORIDES;
D O I
10.1016/j.poly.2014.09.029
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The N-(diferrocenylmethylene)aniline Schiff base Fc(2)C = NPh (1) (Fc = ferrocenyl, Ph = phenyl) was synthesized by the reaction of diferrocenyl-methanone with aniline, and its structure was determined for the first time in this paper. The crystal structure of the novel cyclopalladated complex (Fc(2)C = NPh)PdClPPh3 (2) was analyzed by single crystal X-ray diffraction. The structure of ligand 1 displays an anti-configuration for the ferrocenyl groups bonded to the C atom of the C=N bond lying on the opposite side to the phenyl ring. The structure of complex 2 shows a four-coordinated structural type and the two ferrocenyl moieties bridged through the C atom of the C=N bond remain in the anti-configuration; the structure also contains a bicyclic system of the coordinated Cp ring and a five-membered metallacycle. The electrochemical properties of ligand 1 and complex 2 were studied by cyclic voltammetry, and the results reveal that there is a stronger electronic communication between the two ferrocenyl units in 2. The results of a catalytic evaluation show that complex 2 is highly active as a catalyst for the Suzuki C-C coupling reaction and the biphenyl product gotten in this reaction can be obtained in 93% yield. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:621 / 626
页数:6
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